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ETFDH Polyclonal antibody

ETFDH Polyclonal Antibody for IHC, IP, WB, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, IP, IHC, IF, ELISA

Conjugate

Unconjugated

Cat no : 11109-1-AP

Synonyms

ETF dehydrogenase, ETF QO, ETF ubiquinone oxidoreductase, ETFDH, ETFQO, MADD



Tested Applications

Positive WB detected inmouse brain tissue, HEK-293 cells, rat brain tissue, mouse kidney tissue, mouse skeletal muscle tissue, rat kidney tissue
Positive IP detected inmouse brain tissue
Positive IHC detected inhuman liver cancer tissue, human liver tissue, human kidney tissue, human prostate cancer tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:1000-1:6000
Immunoprecipitation (IP)IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate
Immunohistochemistry (IHC)IHC : 1:50-1:500
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

11109-1-AP targets ETFDH in WB, IP, IHC, IF, ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Reactivity human, mouse, rat
Cited Reactivityhuman, mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen ETFDH fusion protein Ag1568
Full Name electron-transferring-flavoprotein dehydrogenase
Calculated Molecular Weight 64 kDa
Observed Molecular Weight 64 kDa
GenBank Accession NumberBC011890
Gene Symbol ETFDH
Gene ID (NCBI) 2110
RRIDAB_2231382
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Background Information

ETFDH(Electron transfer flavoprotein-ubiquinone oxidoreductase, mitochondrial) is also named as ETF-QO and belongs to the ETF-QO/fixC family.It is a 64-kDa monomer integrated in the inner mitochondrial membrane, con- tains one molecule of FAD and a 4Fe4S cluster(PMID:12815589).Defects in ETFDH are the cause of glutaric aciduria type 2C (GA2C).This antibody is speicific to ETFDH.

Protocols

Product Specific Protocols
WB protocol for ETFDH antibody 11109-1-APDownload protocol
IHC protocol for ETFDH antibody 11109-1-APDownload protocol
IP protocol for ETFDH antibody 11109-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
human,mouseWB

Ann Neurol

Both ETFDH mutations and FAD homeostasis disturbance are essential for developing riboflavin-responsive multiple Acyl-CoA dehydrogenation deficiency.

Authors - Jingwen Xu
mouseWB

Cell Mol Life Sci

Mitochondrial FAD shortage in SLC25A32 deficiency affects folate-mediated one-carbon metabolism.

Authors - Min-Zhi Peng
humanWB

Hum Mol Genet

Clinical, pathological and genetic features and follow-up of 110 patients with late-onset MADD: A single-center retrospective study.

Authors - Bing Wen
humanWB

J Neurol Neurosurg Psychiatry

Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations.

Authors - Wen Bing B
humanWB,IF

Front Oncol

Propofol Inhibits Proliferation and Augments the Anti-Tumor Effect of Doxorubicin and Paclitaxel Partly Through Promoting Ferroptosis in Triple-Negative Breast Cancer Cells.

Authors - Chen Sun
humanWB

J Mol Med (Berl)

Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A.

Authors - Wang Zhi-Qiang ZQ